Crazy Nanna Hazel & Evie
16 July 2024
My granddaughter Evie Mae, who is four, was diagnosed with NF1 last year.
This happened after her mum, Charlotte, took her to hospital with concerns about her right eye.
Evie was soon told she had Optic Pathway Gliomas on both eyes, blind in her right eye, and is now undergoing a 19 month programme of chemotherapy to try and save the sight in her left eye.
There is no family history of NF1 on either side.
We all did some research into NF1 to find out more on this disease.
– Hazel"We came across Nerve Tumours UK, the information and the support available was so invaluable. The devastation, sadness and shock that your little granddaughter is so poorly, there is huge comfort knowing I could find out answers to my questions and know there is support if I need it."
I wanted to fundraise for Nerve Tumours UK to raise more awareness and to help and support other families that are going through similar journeys. In my mind I thought of doing "something different."
My granddaughters have always called me "Crazy Nanna" due to me having a great sense of fun!
Why not be crazy??
Then I booked the Skydive.
Evie has been so brave, surely I can be brave too.
My heart was in pieces when I was told of the NF1 diagnosis, and that worse still, there is no cure.....it is and always will be WHY???
I have to be the best Nanna I can be.
I'm here to encourage, love and support her unconditionally, through whatever is thrown at Evie, big sister Ava and their parents, now and in the future.
Evie loves spending time with me: planting flowers; Playdoh; she's great at washing up and pillow fights too.
I'm "Crazy Nanna", sharing huge love and squeezy hugs with my feisty little "Ginger Ninja".
You can read more about Evie, in her mother Charlotte's story: https://nervetumours.org.uk/news/charlottes-evies-story